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门诊外周神经连续阻滞治疗截肢后幻肢痛:一项多中心、随机、四盲、安慰剂对照临床试验。

Ambulatory continuous peripheral nerve blocks to treat postamputation phantom limb pain: a multicenter, randomized, quadruple-masked, placebo-controlled clinical trial.

机构信息

Department of Anesthesiology, University of California San Diego, San Diego, CA, United States.

Outcomes Research Consortium, Cleveland, OH, United States.

出版信息

Pain. 2021 Mar 1;162(3):938-955. doi: 10.1097/j.pain.0000000000002087.

DOI:10.1097/j.pain.0000000000002087
PMID:33021563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7920494/
Abstract

Phantom limb pain is thought to be sustained by reentrant neural pathways, which provoke dysfunctional reorganization in the somatosensory cortex. We hypothesized that disrupting reentrant pathways with a 6-day-long continuous peripheral nerve block reduces phantom pain 4 weeks after treatment. We enrolled patients who had an upper- or lower-limb amputation and established phantom pain. Each was randomized to receive a 6-day perineural infusion of either ropivacaine or normal saline. The primary outcome was the average phantom pain severity as measured with a Numeric Rating Scale (0-10) at 4 weeks, after which an optional crossover treatment was offered within the following 0 to 12 weeks. Pretreatment pain scores were similar in both groups, with a median (interquartile range) of 5.0 (4.0, 7.0) for each. After 4 weeks, average phantom limb pain intensity was a mean (SD) of 3.0 (2.9) in patients given local anesthetic vs 4.5 (2.6) in those given placebo (difference [95% confidence interval] 1.3 [0.4, 2.2], P = 0.003). Patients given local anesthetic had improved global impression of change and less pain-induced physical and emotional dysfunction, but did not differ on depression scores. For subjects who received only the first infusion (no self-selected crossover), the median decrease in phantom limb pain at 6 months for treated subjects was 3.0 (0, 5.0) vs 1.5 (0, 5.0) for the placebo group; there seemed to be little residual benefit at 12 months. We conclude that a 6-day continuous peripheral nerve block reduces phantom limb pain as well as physical and emotional dysfunction for at least 1 month.

摘要

幻肢痛被认为是由折返神经通路维持的,这些通路会引起躯体感觉皮层的功能失调重组。我们假设,通过为期 6 天的连续外周神经阻滞来破坏折返通路,可以在治疗后 4 周减轻幻肢痛。我们招募了有上肢或下肢截肢并伴有幻肢痛的患者。每位患者都被随机分配到接受罗哌卡因或生理盐水为期 6 天的周围神经输注。主要结局是在 4 周时用数字评分量表(0-10)测量的平均幻肢痛严重程度,之后在接下来的 0-12 周内提供可选的交叉治疗。两组患者的预处理疼痛评分相似,分别为 5.0(4.0,7.0)。4 周后,接受局部麻醉的患者平均幻肢痛强度为 3.0(2.9),而接受安慰剂的患者为 4.5(2.6)(差异[95%置信区间]为 1.3[0.4, 2.2],P = 0.003)。接受局部麻醉的患者在整体变化印象和减轻疼痛引起的身体和情绪功能障碍方面有改善,但抑郁评分无差异。对于仅接受第一次输注(无自我选择交叉)的患者,治疗组在 6 个月时幻肢痛的中位数下降为 3.0(0,5.0),安慰剂组为 1.5(0,5.0);12 个月时似乎没有明显的残留获益。我们的结论是,为期 6 天的连续外周神经阻滞可减轻幻肢痛以及至少 1 个月的身体和情绪功能障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4311/7920494/3a7144aaf937/jop-162-938-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4311/7920494/50888b56ea95/jop-162-938-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4311/7920494/23a2edc50ad5/jop-162-938-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4311/7920494/1b768ec05dcc/jop-162-938-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4311/7920494/ccffbe52bb54/jop-162-938-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4311/7920494/3a7144aaf937/jop-162-938-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4311/7920494/50888b56ea95/jop-162-938-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4311/7920494/23a2edc50ad5/jop-162-938-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4311/7920494/1b768ec05dcc/jop-162-938-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4311/7920494/ccffbe52bb54/jop-162-938-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4311/7920494/3a7144aaf937/jop-162-938-g005.jpg

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